Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Daji Chen"'
Autor:
Daji Chen, Linlin Wan, Zhao Chen, Xinrong Yuan, Mingjie Liu, Zhichao Tang, You Fu, Sudan Zhu, Xuewei Zhang, Rong Qiu, Beisha Tang, Hong Jiang
Publikováno v:
Frontiers in Aging Neuroscience, Vol 14 (2023)
AimThere is increasing evidence suggesting that vitamins may play important roles in the pathogenesis of multiple system atrophy (MSA). The purpose of this study was to detect the changes of serum vitamin levels and investigate their correlation with
Externí odkaz:
https://doaj.org/article/cd01f8215cd54c9fb744daea39b045cd
Autor:
Linliu Peng, Linlin Wan, Mingjie Liu, Zhe Long, Daji Chen, Xinrong Yuan, Zhichao Tang, You Fu, Sudan Zhu, Lijing Lei, Chunrong Wang, Huirong Peng, Yuting Shi, Lang He, Hongyu Yuan, Na Wan, Xuan Hou, Kun Xia, Jinchen Li, Chao Chen, Rong Qiu, Beisha Tang, Zhao Chen, Hong Jiang
Publikováno v:
Journal of Neurology.
Autor:
Zhao Chen, Guang Liao, Na Wan, Zhiyou He, Daji Chen, Zhichao Tang, Zhe Long, Guangdong Zou, Linliu Peng, Linlin Wan, Chunrong Wang, Huirong Peng, Yuting Shi, Yongxiang Tang, Jian Li, Yulai Li, Tingting Long, Xuan Hou, Lang He, Rong Qiu, Dengming Chen, Junling Wang, Jifeng Guo, Lu Shen, Yiyun Huang, Tetsuo Ashizawa, Thomas Klockgether, Beisha Tang, Ming Zhou, Shuo Hu, Hong Jiang
Publikováno v:
Movement disorders 38(6), 978-989 (2023). doi:10.1002/mds.29395
Severe reduced synaptic density was observed in spinocerebellar ataxia (SCA) in postmortem neuropathology, but in vivo assessment of synaptic loss remains challenging. OBJECTIVE SPINOCEREBELLAR ATAXIA TYPE 3: The objective of this study was to assess
Autor:
Mingjie Liu, Linlin Wan, Chunrong Wang, Hongyu Yuan, Yun Peng, Na Wan, Zhichao Tang, Xinrong Yuan, Daji Chen, Zhe Long, Yuting Shi, Rong Qiu, Beisha Tang, Hong Jiang, Zhao Chen
Publikováno v:
Genes & Genomics. 44:1061-1070
Coffin-Siris syndrome (CSS) is a rare congenital syndrome characterized by developmental delay, intellectual disability, microcephaly, coarse face and hypoplastic nail of the fifth digits. Heterozygous variants of different BAF complex-related genes